Evidence map›Paper›PMID 39010703›Full record

ArticleClinical and translational science2024

The effect of itraconazole, a strong CYP3A4 inhibitor, on the pharmacokinetics of the first-in-class ACKR3/CXCR7 antagonist, ACT-1004-1239.

Christine Huynh, Jasper Dingemanse, Henriette E Meyer Zu Schwabedissen, Marlene Fonseca, Patricia N Sidharta

Abstract readClinical Trial, Phase I
In one paragraph

Article in Clinical and translational science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Christine HuynhDepartment of Clinical Pharmacology, Idorsia Pharmaceuticals Ltd, Allschwil, Switzerland.ORCID 0000-0003-2468-7305
Jasper DingemanseDepartment of Clinical Pharmacology, Idorsia Pharmaceuticals Ltd, Allschwil, Switzerland.ORCID 0000-0002-4083-5817
Henriette E Meyer Zu SchwabedissenDepartment of Pharmaceutical Sciences, Biopharmacy, University of Basel, Basel, Switzerland.ORCID 0000-0003-0458-4579
Marlene FonsecaBlueClinical Phase 1, Hospital de Prelada, Porto, Portugal.ORCID 0009-0000-5828-8535
Patricia N SidhartaDepartment of Clinical Pharmacology, Idorsia Pharmaceuticals Ltd, Allschwil, Switzerland.ORCID 0000-0001-7581-4525

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytochrome P450 (CYP) 3A4 is an enzyme involved in the metabolism of many drugs that are currently on the market and is therefore a key player in drug-drug interactions (DDIs). ACT-1004-1239 is a potent and selective, first-in-class ACKR3/CXRC7 antagonist being developed as a treatment for demyelinating diseases including multiple sclerosis. Based on the human absorption, distribution, metabolism, and excretion (ADME) study results, ACT-1004-1239 is predominantly metabolized by CYP3A4. This study investigated the effect of the strong CYP3A4 inhibitor, itraconazole, on the pharmacokinetics of single-dose ACT-1004-1239 in healthy male subjects. In the open-label, fixed-sequence DDI study, a total of 16 subjects were treated. Each subject received a single dose of 10 mg ACT-1004-1239 (Treatment A) in the first period followed by concomitant administration of multiple doses of 200 mg itraconazole and a single dose of 10 mg ACT-1004-1239 in the second period. We report a median of difference in t

Indexed as

Cytochrome P-450 CYP3ACytochrome P-450 CYP3A InhibitorsDrug InteractionsItraconazoleAdultArea Under CurveHealthy VolunteersHumansMaleMiddle AgedYoung AdultCYP3A4 protein, humanCytochrome P-450 CYP3ACytochrome P-450 CYP3A InhibitorsItraconazole

Identifiers

PMID39010703
PMCPMC11249824

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.